EP3387904A1 - Compositions herbicides contenant du sulfonylurea liquide - Google Patents

Compositions herbicides contenant du sulfonylurea liquide Download PDF

Info

Publication number
EP3387904A1
EP3387904A1 EP18170343.0A EP18170343A EP3387904A1 EP 3387904 A1 EP3387904 A1 EP 3387904A1 EP 18170343 A EP18170343 A EP 18170343A EP 3387904 A1 EP3387904 A1 EP 3387904A1
Authority
EP
European Patent Office
Prior art keywords
methyl
ethyl
tribenuron
metsulfuron
sulfonylurea
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
EP18170343.0A
Other languages
German (de)
English (en)
Other versions
EP3387904B1 (fr
Inventor
Oliver Egan
Andrew Goldsmith
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Battelle UK Ltd
Mitsui AgriScience International NV SA
Original Assignee
Battelle UK Ltd
Mitsui AgriScience International NV SA
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Battelle UK Ltd, Mitsui AgriScience International NV SA filed Critical Battelle UK Ltd
Priority to PL18170343T priority Critical patent/PL3387904T3/pl
Publication of EP3387904A1 publication Critical patent/EP3387904A1/fr
Application granted granted Critical
Publication of EP3387904B1 publication Critical patent/EP3387904B1/fr
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
    • A01N25/02—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests containing liquids as carriers, diluents or solvents
    • A01N25/04—Dispersions, emulsions, suspoemulsions, suspension concentrates or gels
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
    • A01N25/22—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests containing ingredients stabilising the active ingredients
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
    • A01N25/30—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests characterised by the surfactants
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
    • A01N43/40—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom six-membered rings
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
    • A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
    • A01N47/28—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N<
    • A01N47/36—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N< containing the group >N—CO—N< directly attached to at least one heterocyclic ring; Thio analogues thereof
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N59/00—Biocides, pest repellants or attractants, or plant growth regulators containing elements or inorganic compounds
    • A01N59/04—Carbon disulfide; Carbon monoxide; Carbon dioxide
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N59/00—Biocides, pest repellants or attractants, or plant growth regulators containing elements or inorganic compounds
    • A01N59/06—Aluminium; Calcium; Magnesium; Compounds thereof
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N59/00—Biocides, pest repellants or attractants, or plant growth regulators containing elements or inorganic compounds
    • A01N59/08—Alkali metal chlorides; Alkaline earth metal chlorides
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N59/00—Biocides, pest repellants or attractants, or plant growth regulators containing elements or inorganic compounds
    • A01N59/26—Phosphorus; Compounds thereof

Definitions

  • This invention relates to liquid herbicidal compositions comprising a non-aqueous solvent system, at least one sulfonylurea herbicide and at least one inorganic salt selected from the metal carbonates and metal phosphates.
  • the invention also relates to the use of an inorganic salt selected from the metal carbonates and metal phosphates to improve chemical stabilisation of sulfonylurea herbicides in liquid compositions that comprise non-aqueous solvent systems.
  • Typical liquid formulations include oil-based formulations such as oil dispersions (OD), emulsifiable concentrates (EC), and soluble concentrates (SL) where one or more active ingredients are dissolved in and/or suspended in the liquid media of the formulation.
  • OD oil dispersions
  • EC emulsifiable concentrates
  • SL soluble concentrates
  • Sulfonylureas are a well-known and important class of herbicides comprising more than 30 active-ingredients that are widely used for controlling a range of annual and perennial broadleaved weeds and grasses in a wide variety of agricultural and horticultural crops, as well as in turf, pastures and non-crop situations.
  • sulfonylureas are known to be unstable as they have a tendency to hydrolyse via cleavage at the sulfonylurea bridge. While this instability is sometimes considered favourable in terms of achieving low soil residues of these compounds, it poses serious problems commercially with respect to the storage stability of the formulated products.
  • US 2006/0276337 A1 (Bayer CropScience GmbH) describes an oil suspension concentrate comprising one or more pyridylsulfonylurea compounds suspended in one or more organic solvents optionally with a sulfosuccinate salt.
  • the oil suspensions are reported to be storage-stable but no quantitative measurement regarding stability is provided.
  • WO 2007/027863 A2 (E.I. du Pont de Nemours & Co.) is also concerned with providing stable sulfonylurea-containing liquid compositions and describes an oil suspension concentrate comprising one or more sulfonylurea herbicides, additionally one or more fatty acid esters of C1-C4 alkanols, and a lignosulfonate.
  • the stability of these compositions was found to vary dependent on the sulfonylurea that was used.
  • the document is concerned with providing stable compositions, up to 66.5% of tribenuron-methyl was lost after only one week of storage at 40°C.
  • US 5,731,264 (ISP Investments Inc.) describes a liquid emulsifiable concentrate comprising a sulfonylurea and a mixture of anionic and non-ionic surfactants dissolved in a solvent selected from gamma-butyrolactone, propylene glycol or propylene carbonate or mixtures thereof.
  • a solvent selected from gamma-butyrolactone, propylene glycol or propylene carbonate or mixtures thereof.
  • the obtained formulations comprising metsulfuron- methyl which is considered to be of average stability, are reported to have a half-life of 5.8 days at 52°C. After 5 days, between 25-30% of the metsulfuron methyl was lost depending on the selected solvent.
  • WO 2008/155108 A2 (GAT Microencapsulation AG) describes oil suspensions of sulfonylureas and organomodified silane compounds that are reportedly stable when stored at comparatively gentle accelerated storage conditions of 35°C for 15 days.
  • WO 2009/152827 A2 also GAT Microencapsulation AG
  • the more usual accelerated storage conditions of 54°C for two weeks are used but in this document the chemical stability of the sulfonylurea in the suspension concentrates is not reported.
  • EP 0554015 A1 (Ishihara Sangyo Kaisha, Ltd.) describes a chemically stabilized herbicidal oil-based suspension, comprising N-[(4,6-dimethoxypyrimidin-2-yl) aminocarbonyl-3-dimethylaminocarbonyl-2-pyridinesulfonamide and/or its salt as an effective herbicidal component, urea, a vegetable oil and/or mineral oil, a surfactant and, optionally other ingredients such as an additional herbicidal component, a thickener, a solvent and other adjuvants.
  • urea is added to suppress decomposition of the effective herbicidal component and to provide a chemically stabilized herbicidal oil-based suspension.
  • GB 2496643 A (Rotam Agrochem International Company Ltd.) aims to improve the suspension concentrate described in EP 0554015 A1 .
  • This document is concerned with pyridine sulfonamides (i.e. pyridylsulfonylureas) and teaches to add a polyether-polysiloxane to the composition to counteract supposed poor spreading and water dispersibility caused by the addition of urea or other stabilizers to a suspension concentrate.
  • EP 0 124 295 A2 reports that aqueous suspensions of sulfonylureas can be stabilized by the presence of ammonium, substituted ammonium or alkali metal salts of carboxylic acid or inorganic acid provided that the salts exhibit specific solubility and pH properties.
  • Exemplary salts are said to be diammonium hydrogen phosphate, ammonium acetate, lithium acetate, sodium acetate, potassium acetate, or sodium thiocyanate.
  • WO 03/051114 A1 (ISP Investments Inc.) is concerned with increasing the shelf - life of an oil-in-water microemulsion containing a biologically active aza type compound.
  • the oil-in-water microemulsion contains from 90 to 99.99 wt.% water. Shelf - life is said to be extended by the addition of a buffering agent to the emulsion.
  • the buffering agent is an alkaline buffering agent such as an inorganic Na, K and or NH 4 salt of a phenol, a polyphenol or a weak acid; an alkanol amine; a polyamine salt of a weak acid or a mixture of these buffering agents. No stability data is provided for any sulfonylurea-containing formulations.
  • WO 2013/174833 A1 (Bayer CropScience AG) describes an oil dispersion formulation of iodosulfuron-methyl sodium salt which comprise hydroxystearates, in particular lithium hydroxystearate as both a thickener and a stabilizer for the sulfonylurea.
  • the present invention is based on the surprising finding that the chemical stability of many sulfonylureas in liquid composition comprising a non-aqueous solvent system can be improved by incorporating an inorganic salt selected from the metal carbonates and metal phosphates into the composition.
  • the present invention relates to liquid herbicidal compositions comprising: a non-aqueous solvent system; at least one sulfonylurea herbicide; and at least one inorganic salt selected from the metal carbonates and metal phosphates.
  • the inorganic salt preferably comprises a metal selected from Na, K, Ca, Mg or Al and/or is an inorganic salt selected from the alkali metal phosphates and the alkali metal carbonates.
  • Preferred inorganic salts are Na 3 PO 4 , K 3 PO 4 , Mg 3 (PO 4 ) 2 , AlPO 4 , and Na 2 CO 3 .
  • the present invention is suitable for chemically stabilising liquid compositions comprising one, two, three, four or more different sulfonylurea compounds.
  • the liquid herbicidal composition is preferably formulated as an oil dispersion (OD), a dispersible concentrate (DC), an emulsifiable concentrate (EC), or a soluble concentrate (SL).
  • OD oil dispersion
  • DC dispersible concentrate
  • EC emulsifiable concentrate
  • SL soluble concentrate
  • At least one sulfonylurea is dissolved, suspended or otherwise contained in the non-aqueous solvent system.
  • At least one inorganic salt selected from the metal carbonates and metal phosphates is dissolved, suspended or otherwise contained in the non-aqueous solvent system.
  • the liquid herbicidal composition of the invention may comprise one or more non-sulfonylurea herbicides that are suspended, dissolved or otherwise contained in the non-aqueous solvent system.
  • the present invention is particularly suitable for improving the chemical stability of a sulfonylurea in the presence of a non-sulfonylurea herbicide that would ordinarily impair its chemical stability.
  • the liquid herbicidal composition may comprise one or more safeners.
  • the liquid herbicidal composition may also comprise co-formulants such as surfactants, particularly non-ionic surfactants.
  • the invention also relates to the use of an inorganic salt selected from the metal carbonates and metal phosphates to improve chemical stabilisation of a sulfonylurea herbicide in a liquid composition that comprises a non-aqueous solvent system.
  • the terms “comprises”, “comprising”, “includes”, “including”, “has”, “having” or any other variation thereof are intended to cover a non-exclusive inclusion.
  • a composition that comprises a list of components is not necessarily limited to only those components but may include other components that are not expressly listed or inherent to such a composition. That said, the terms “comprises”, “comprising”, “includes”, “including”, “has”, “having” or any other variation thereof also cover the disclosed embodiment having no further additional components (i.e. consisting of those components).
  • compositions comprising a sulfonylurea, an inorganic salt, an organic solvent, and a surfactant discloses the composition with just these four components as well as compositions comprising these four components along with other unmentioned components.
  • the herbicidal composition of the invention is a liquid.
  • liquid is meant that the composition takes the form of a liquid at standard temperature and pressure.
  • suitable liquid compositions include the oil-based liquid formulations defined in the " Catalogue of pesticide formulation types and international coding system", Technical Monograph No. 2, 6th Ed. May 2008, CropLife International .
  • Exemplary liquid compositions for use in the present invention include a dispersible concentrate (DC), an emulsifiable concentrate (EC), the liquid part(s) of a solid/liquid (KK) or liquid/liquid (KL) combi-pack, an oil dispersion (OD), an oil miscible flowable concentrate (OF), an oil miscible liquid (OL), an oil-based soluble concentrate (SL), a spreading oil (SO), an oil-based ultra-low volume liquid (UL) or suspension (SU), or any other oil-based liquid not yet designated by a specific code in the CropLife monograph (AL).
  • oil dispersions (OD), dispersible concentrates (DC), emulsifiable concentrates (EC), and oil-based soluble concentrates (SL) are preferred.
  • the invention is particularly suited to improving the chemical stability of sulfonylureas in oil dispersions (OD), emulsifiable concentrates (EC), and soluble concentrates (SL). Accordingly, these types of formulation are the most preferred for the present invention.
  • oil dispersion is to be understood as meaning a dispersion concentrate based on a non-aqueous solvent in which one or more solid active compounds are suspended and wherein further active ingredients are optionally dissolved in the non-aqueous solvent.
  • at least one sulfonylurea compound is suspended in the non-aqueous solvent system. Additional sulfonylurea compounds may be co-suspended and/or dissolved in the non-aqueous solvent system.
  • one or more non-sulfonylurea herbicidal compounds may be suspended and/or dissolved in the non-aqueous solvent system.
  • the inorganic salt is also suspended in the non-aqueous solvent system.
  • the terms " suspended " and " dissolved “ take their ordinary meaning in this technical field. Whether a compound is suspended or dissolved can be determined at standard temperature and pressure.
  • the term " suspended " can be taken to mean that 80 wt.% or more, preferably 90 wt.% or more, even more preferably 95 wt.% or more of the compound in question is suspended within the liquid composition whereas the term “ dissolved " can be taken to mean that 90 wt.% or more, preferably 95 wt.% or more, even more preferably 99 wt.% or more of the compound in question is dissolved in the liquid composition.
  • the liquid composition of the present invention comprises a sulfonylurea.
  • the sulfonylurea is not particularly limited and can be any herbicidal sulfonylurea known in the art or described in the patent literature.
  • the sulfonylurea may be selected from the sulfonylureas listed in the 16th Edition of "The Pesticide Manual" (ISBN-10: 190139686X ).
  • the sulfonylurea may be a compound according to Formula (I) as described in WO 2007/027863 A2 (E.I. DuPont De Nemours and Company): wherein J is R 13 SO 2 N(CH 3 )- or J is selected from the group consisting of and wherein:
  • alkyl used either alone or in compound words such as “alkylthio” or “haloalkyl” includes a straight-chain or branched alkyl, such as, methyl, ethyl, n- propyl, i -propyl, or the different butyl isomers;
  • cycloalkyl includes, for example, cyclopropyl, cyclobutyl and cyclopentyl;
  • alkenyl includes straight-chain or branched alkenes such as ethenyl, 1-propenyl, 2-propenyl, and the different butenyl isomers;
  • alkenyl also includes polyenes such as 1,2-propadienyl and 2,4-butadienyl;
  • alkynyl includes straight-chain or branched alkynes such as ethynyl, 1-propynyl, 2-propynyl and the different butynyl is
  • Cj-Cj the total number of carbon atoms in a substituent group is indicated by the "Cj-Cj" prefix where i and j are numbers from 1 to 5.
  • C 1 -C 4 alkyl designates methyl through butyl, including the various isomers.
  • C 2 alkoxyalkyl designates CH 3 OCH 2
  • C 3 alkoxyalkyl designates, for example, CH 3 CH(OCH 3 ), CH 3 OCH 2 CH 2 or CH 3 CH 2 OCH 2
  • C 4 alkoxyalkyl designates the various isomers of an alkyl group substituted with an alkoxy group containing a total of four carbon atoms, examples including CH 3 CH 2 CH 2 OCH 2 and CH 3 CH 2 OCH 2 CH 2 .
  • halogen either alone or in compound words such as “haloalkyl” includes fluorine, chlorine, bromine or iodine. Further, when used in compound words such as “haloalkyl”, said alkyl may be partially or fully substituted with halogen atoms which may be the same or different. Examples of “haloalkyl” include F 3 C, ClCH 2 , CF 3 CH 2 and CF 3 CCl 2 .
  • haloalkoxy "haloalkylthio" and the like, are defined analogously to the term “haloalkyl”.
  • haloalkoxy examples include CF 3 O, CCl 3 CH 2 O, HCF 2 CH 2 CH 2 O and CF 3 CH 2 O.
  • haloalkylthio examples include CCl 3 S, CF 3 S, CCl 3 CH 2 S and ClCH 2 CH 2 CH 2 S.
  • preferable sulfonylureas according to Formula (I) include those where X is selected from the group C 1 -C 4 alkyl, C 1 -C 4 alkoxy, C 1 -C 4 haloalkoxy, halogen, di(C 1 -C 3 alkyl)amino and Y is selected from the group C 1 -C 4 alkyl, C 1 -C 4 alkoxy, and C 1 -C 4 haloalkoxy. More preferably, X is selected from CH 3 , OCH 3 , Cl, OCHF 2 , and N(CH 3 ) 2 and Y is selected from CH 3 , OCH 3 , OCHF 2 and OCH 2 CF 3 .
  • Preferable sulfonylureas according to Formula (I) also include those where J is J-1, R 1 is Cl, CO 2 CH 3 , CO 2 C 2 H 5 , CH 2 CH 2 CF 3 , or OCH 2 CH 2 Cl, and R 2 is H; J is J-1, R 1 is CO 2 CH 3 , and R 2 is CH 3 ; J is J-2, R 3 is CO 2 C 2 H 5 , OCH 2 CH 3 , or COC 3 -cycloalkyl, L 1 is CH 2 , O, or NH, and R 2 is H; J is J-5, R 4 is CO 2 CH 3 , and R 5 is H; J is J-6, R 6 is CON(CH 3 ) 2 , SO 2 CH 2 CH 3 , or CF 3 , and R 7 is H; J is J-10, R 8 is CH 3 , R 9 is CO 2 CH 3 and R 10 is Cl.
  • the sulfonylurea according to Formula (I), or any of the exemplary sulfonylureas mentioned herein, is to be understood as meaning all of the usual use forms in this technical field, such as acids, esters, salts and isomers.
  • the salt includes acid-addition salts with inorganic or organic acids such as hydrobromic, hydrochloric, nitric, phosphoric, sulfuric, acetic, butyric, fumaric, lactic, maleic, malonic, oxalic, propionic, salicylic, tartaric, 4-toluenesulfonic or valeric acids.
  • salts formed with organic bases e.g., pyridine, ammonia, or triethylamine
  • inorganic bases e.g., hydrides, hydroxides, or carbonates of sodium, potassium, lithium, calcium, magnesium or barium
  • Preferred salts of the sulfonylureas according to Formula (I), or the exemplary sulfonylureas mentioned herein, include lithium, sodium, potassium, triethylammonium, and quaternary ammonium salts.
  • Preferred esters for the purpose of this invention are the alkyl esters, in particular the C 1 -C 10 -alkyl esters, such as methyl and ethyl esters.
  • Exemplary sulfonylureas according to Formula (I) that can be used for this invention include:
  • sulfonylureas e.g. propyrisulfuron: 2-chloro- N -[[(4,6-dimethoxy-2-pyrimidinyl)amino]carbonyl]-6-propylimidazo[1,2- b ]pyridazine-3-sulfonamide
  • propyrisulfuron 2-chloro- N -[[(4,6-dimethoxy-2-pyrimidinyl)amino]carbonyl]-6-propylimidazo[1,2- b ]pyridazine-3-sulfonamide
  • Preferred salts of the sulfonylureas mentioned above include the sodium salt thereof and the potassium salt thereof.
  • the sulfonylurea is preferably comprised in the liquid compositions of the invention in an amount of at least 0.1 wt.% based on the total weight of the liquid composition. More preferably, the sulfonylurea is comprised in an amount of at least 0.2 wt.%, at least 0.5 wt.%, at least 0.7 wt.%, at least 1 wt.%, at least 2 wt.%, at least 5 wt.% or at least 7 wt.%. The sulfonylurea is preferably comprised in the composition in an amount of 60 wt.% or less.
  • the sulfonylurea is comprised in an amount of 50 wt.% or less, 40 wt.% or less, 30 wt.% or less, 25 wt.% or less, 20 wt.% or less, 10 wt.% or less, 5 wt.% or less, 2 wt.% or less, or 1 wt.% or less. Any of the preferred lower wt.% limits for the amount of sulfonylurea can be combined with any of the preferred upper wt.% limits to define further suitable wt.% ranges for the present invention.
  • further exemplary ranges for the amount of sulfonylurea in the liquid composition include 0.1 to 60 wt.%, 1 to 50wt.%, 2 to 40 wt.%, 5 to 30 wt.%, 0.5 to 20 wt.%, 7 to 30 wt.%, 5 to 10 wt.%, 0.2 to 5 wt.%, 0.5 to 2 wt.% and 0.5 to 1 wt.%.
  • the wt.% amounts that are described herein refer to the weight amount of the modified sulfonylurea.
  • the amounts described herein refer to the sum amount of all the sulfonylureas present in the composition.
  • the sulfonylurea has a particle size (D50) of at least 100 nm or more, at least 200 nm or more, at least 500 nm or more, at least 1 ⁇ m or more, at least 2 ⁇ m or more, or at least 3 ⁇ m or more as a particle size less than this can generate excess heat during milling and possibly degrade the sulfonylurea.
  • D50 particle size
  • the sulfonylurea has a particle size (D50) of 30 ⁇ m or less, 15 ⁇ m or less, 10 ⁇ m or less, 7 ⁇ m or less, 5 ⁇ m or less, 3 ⁇ m or less, 1 ⁇ m or less, 500 nm or less.
  • D50 particle size
  • Any of the preferred lower limits for the sulfonylurea particle size can be combined with any of the preferred upper limits to define further suitable particle size ranges for the present invention.
  • further exemplary ranges for the particle size (D50) of the sulfonylurea include 0.1-30 ⁇ m, 0.2-15 ⁇ m, 0.5-10 ⁇ m, 0.1-0.5 ⁇ m, 0.2-1 ⁇ m, 0.5-3 ⁇ m, 1-15 ⁇ m, 1-10 ⁇ m, 1-7 ⁇ m, 2-15 ⁇ m, 2-10 ⁇ m, 2-7 ⁇ m, 3-15 ⁇ m, 3-10 ⁇ m, and 3-7 ⁇ m.
  • D50 refers to the volume median particle size and can be determined by laser light scattering using the method described in CIPAC MT187.
  • the liquid composition of the invention may comprise more than one sulfonylurea herbicide compound.
  • the liquid composition may comprise any combination of sulfonylureas as disclosed herein.
  • the liquid composition may comprise tribenuron-methyl and any other sulfonylurea described herein; the liquid composition may comprise metsulfuron-methyl and any other sulfonylurea described herein; or the liquid composition may comprise nicosulfuron and any other sulfonylurea described herein.
  • the liquid herbicidal composition comprises at least one sulfonylurea that is not a pyridylsulfonylurea. In another aspect of the invention the herbicidal composition does not comprise a pyridylsulfonylurea. In one further aspect of the invention the herbicidal composition does not comprise nicosulfuron.
  • the composition of the present invention comprises at least one inorganic salt selected from the metal phosphates and the metal carbonates.
  • Exemplary metal salts include those derived from the alkali metals such as lithium, sodium and potassium, the alkaline earth metals such as magnesium and calcium, as well as those derived from other metals such as aluminium.
  • Preferred salts for the present invention include sodium phosphate and sodium carbonate in their various forms.
  • Exemplary salts include Na 3 PO 4 , Na 2 CO 3 , AlPO 4 , Mg 3 (PO 4 ) 2 and Na 2 HPO 4 . Both the anhydrous and hydrated forms of the metal salts can be used but the anhydrous form is most preferred in view of improving chemical stability of the sulfonylurea.
  • sodium phosphate and the term “ potassium phosphate” includes the various forms of sodium phosphate and potassium phosphate, respectively, as well as all anhydrous and hydrated forms thereof.
  • sodium phosphate includes monosodium phosphate (anhydrous), monosodium phosphate (monohydrate), monosodium phosphate (dihydrate), disodium phosphate (anhydrous), disodium phosphate (dihydrate), disodium phosphate (heptahydrate), disodium phosphate (octahydrate), disodium phosphate (dodecahydrate), trisodium phosphate (anhydrous, hexagonal), trisodium phosphate (anhydrous, cubic), trisodium phosphate (hemihydrate), trisodium phosphate (hexahydrate), trisodium phosphate (octahydrate), trisodium phosphate (dodecahydrate), monosodium diphosphate (anhydrous), diso
  • trisodium phosphate and tripotassium phosphate provide for a sulfonylurea with superior chemical stability than many of the other salts mentioned herein, particularly with respect to those sulfonylureas that are more prone to hydrolysis in liquid compositions.
  • tribenuron-methyl was found to have excellent chemical stability in the presence of trisodium phosphate.
  • trisodium phosphate in its anhydrous or hydrated forms is particularly preferred as the inorganic salt of the invention.
  • the invention also relates to formulations, as described herein, comprising the above preferred combination of salt and sulfonylurea.
  • the invention also relates to the use of Na 3 PO 4 to improve chemical stabilisation of tribenuron-methyl, metsulfuron-methyl, nicosulfuron, bensulfuron-methyl, foramsulfuron, pyrazosulfuron-ethyl, chlorsulfuron, amidosulfuron, or triasulfuron in all such formulations; or the use of Na 2 CO 3 to improve chemical stabilisation of tribenuron-methyl or nicosulfuron in all such formulations; or the use of Mg 3 (PO 4 ) 2 to improve chemical stabilisation of rimsulfuron, bensulfuron-methyl, mesosulfuron-methyl, thifensulfuron-methyl, chlorimuron-ethyl, or triasulfuron in all such formulations; or the use of AlPO 4 to improve chemical
  • the inorganic salt is preferably comprised in the liquid composition of the invention in an amount of at least 0.01 wt.% based on the total weight of the liquid composition. More preferably, the inorganic salt is comprised in an amount of at least 0.03 wt.%, at least 0.05 wt.%, at least 0.1 wt.%, at least 0.2 wt.%, at least 0.5 wt.%, at least 1 wt.%, at least 2 wt.%.
  • the inorganic salt is preferably comprised in the composition in an amount of 30 wt.% or less to reduce physical stability problems of the formulation and to reduce interference with the function of any surfactants that are optionally present. More preferably, the inorganic salt is comprised in an amount of 25 wt.% or less, 20 wt.% or less, 15 wt.% or less, 10 wt.% or less, 8 wt.% or less, 6 wt.% or less, 5 wt.% or less, 2 wt.% or less, 1 wt.% or less, or 0.7 wt.% or less.
  • any of the preferred lower wt.% limits for the amount of inorganic salt can be combined with any of the preferred upper wt.% limits to define further suitable wt.% ranges for the present invention.
  • further exemplary ranges for the amount of inorganic salt in the liquid composition include 0.01 to 30 wt.%, 0.1 to 25 wt.%, 1 to 20 wt.%, 1 to 10 wt.%, 0.5 to 10 wt.%, 1 to 5 wt.%, 0.5 to 5 wt.%, 0.1 to 2 wt.%, 0.2 to 2 wt.%, 0.2 to 1 wt.%, and 0.2 to 0.7 wt.%.
  • the weight ranges above refer to the total amount of inorganic salt selected from the metal phosphates and metal carbonates that is present in the liquid compositions.
  • the weight ranges above do not refer to other salts that might be present in the composition such as the salt of a sulfonylurea.
  • the amounts described herein refer to the sum amount of all the inorganic salts selected from the metal phosphates and metal carbonates that are present in the composition.
  • the weight ratio of the inorganic salt to sulfonylurea is 0.1 or greater.
  • the weight ratio of the inorganic salt to sulfonylurea is 0.2 or greater, 0.3 or greater, 0.5 or greater, 0.7 or greater, or 1 or greater.
  • the weight ratio of the inorganic salt to sulfonylurea is preferably 5 or less, 4 or less, 3 or less, 2 or less, or 1 or less.
  • the preferred weight ratios refer to the total amount of the inorganic salt selected from the metal phosphates and metal carbonates to the total amount of sulfonylurea compounds in the liquid composition.
  • any of the preferred lower weight ratio limits can be combined with any of the preferred upper weight ratio limits to define further suitable weight ratio ranges for the present invention.
  • further exemplary ranges for the weight ratio of the inorganic salt to sulfonylurea include 0.1 to 5, 0.2 to 4, 0.3 to 3, 0.3 to 1, 0.5 to 2, 0.7 to 2, 0.1 to 2, 1 to 2 and 1 to 5.
  • the total amount of sulfonylurea compounds is 2 to 20 wt.%
  • the total amount of inorganic salt selected from the metal carbonates and metal phosphates is 1 to 20 wt.%
  • the weight ratio of inorganic salt to sulfonylurea is in the range of from 0.1 to 5.
  • the total amount of sulfonylurea compounds is 2 to 20 wt.%
  • the total amount of inorganic salt selected from the metal carbonates and metal phosphates is 1 to 20 wt.%
  • the weight ratio of inorganic salt to sulfonylurea is in the range of from 0.5 to 2.5, preferably 0.7 to 2.3.
  • the weight ratio of Na 2 CO 3 to sulfonylurea is preferably in the range of from 0.1 to 2, more preferably in the range of from 0.1 to 1. If the salt includes Na 3 PO 4 (anhydrous or hydrated) then the weight ratio Na 3 PO 4 to sulfonylurea is preferably in the range of from 0.1 to 2, more preferably in the range of from 0.5 to 2, and most preferably in the range of from 1 to 2.
  • the weight ratio K 3 PO 4 to sulfonylurea is preferably in the range of from 0.1 to 2, more preferably in the range of from 0.5 to 2, and most preferably in the range of from 1 to 2.
  • the particle size (D50) of the inorganic salt is preferably at least 100 nm or more, at least 200 nm or more, at least 500 nm or more, at least 1 ⁇ m or more, at least 1.5 ⁇ m or more, or at least 2 ⁇ m or more.
  • the particle size (D50) of the inorganic salt is preferably 30 ⁇ m or less, 15 ⁇ m or less, 10 ⁇ m or less, 5 ⁇ m or less, 3 ⁇ m or less, 1 ⁇ m or less, or 500 nm or less to improve chemical stability of the sulfonylurea in the composition. Any of the preferred lower limits for the inorganic salt particle size can be combined with any of the preferred upper limits to define further suitable salt particle size ranges for the present invention.
  • further exemplary ranges for the particle size of the inorganic salt include 0.1-30 ⁇ m, 0.2-15 ⁇ m, 0.5-10 ⁇ m, 0.1-0.5 ⁇ m, 0.2-1 ⁇ m, 0.5-3 ⁇ m, 1-15 ⁇ m, 1-10 ⁇ m, 1-5 ⁇ m, 1-3 ⁇ m, 1.5-15 ⁇ m, 2-15 ⁇ m, 2-10 ⁇ m, 2-5 ⁇ m, and 2-3 ⁇ m.
  • D50 refers to the volume median particle size and can be determined by laser light scattering using the method described in CIPAC MT187.
  • the liquid composition comprises at least one inorganic salt selected from the metal carbonates and metal phosphates that is not calcium carbonate or sodium triphosphate. In a further aspect of the invention the liquid composition does not comprise calcium carbonate or sodium triphosphate. In still a further aspect of the invention, if the liquid composition comprises a pyridylsulfonylurea, then the composition does not comprise calcium carbonate or sodium triphosphate. In a further aspect still, if the liquid composition comprises a pyridylsulfonylurea, then the composition does not comprise alkali metal bicarbonates, Na 2 CO 3 or K 2 CO 3 . In still a further aspect of the invention, if the liquid composition comprises nicosulfuron, then the composition does not comprise one or more of calcium carbonate, sodium triphosphate, and alkali metal bicarbonates, Na 2 CO 3 or K 2 CO 3 .
  • the composition of the present invention comprises a non-aqueous solvent system.
  • non-aqueous solvent system means that one or more solvents other than water (e.g. organic solvents) are used as the liquid carrier in the liquid composition. This does not mean to say that the solvent system must necessarily be completely free of water. Trace amounts of water may be present in the components that are used to prepare the non-aqueous solvent system. For instance, trace amounts of water may be introduced into the solvent system by organic solvents, surfactants or salts that are used to prepare the liquid herbicidal composition. While the term " non-aqueous solvent system " is clear in this technical field (e.g.
  • ODs, ECs and SLs employ a non-aqueous solvent system), for the avoidance of any doubt the term can be taken to mean that the liquid composition comprises water in an amount of 5 wt.% or less of the composition, preferably 3 wt.% or less, more preferably 2 wt.% and most preferably 1 wt.% or less.
  • the sulfonylurea and inorganic salt are dissolved, dispersed, suspended or otherwise contained in the non-aqueous solvent system.
  • Typical solvents are described in Marsden, Solvents Guide, 2nd Ed., Interscience, New York, 1950 .
  • the non-aqueous solvent system preferably contains one or more aprotic organic solvents as the major constituent of the solvent system. When the amount of aprotic solvent in the solvent system is 50 wt.% or more, the ability of the inorganic salt to chemically stabilise the sulfonylurea is greatly improved.
  • the one or more aprotic solvents make up 60 wt.% or more, 70 wt.% or more, 80 wt.% or more and most preferably 90 wt.% or more of the solvent system.
  • Suitable aprotic organic solvents for use in the present invention include, for example, those listed under “ Component (C) " in US 2005/0113254 (Bayer CropScience GmbH):
  • fatty acid esters such as C 10 -C 22 -fatty acid esters are glycerol and glycol esters of fatty acids such as C 10 -C 22 -fatty acids, or transesterification products thereof, for example fatty acid alkyl esters such as C 10 -C 22 -fatty acid C 1 -C 20 -alkyl esters, which can be obtained, for example, by transesterification of the abovementioned glycerol or glycol fatty acid esters such as C 10 -C 22 -fatty acid esters with C 1 -C 20 -alcohols (for example methanol, ethanol, propanol or butanol).
  • fatty acid esters such as C 10 -C 22 -fatty acid esters are glycerol and glycol esters of fatty acids such as C 10 -C 22 -fatty acids, or transesterification products thereof, for example fatty acid alkyl esters such as C 10 -C 22 -fatty acid C 1 -
  • Preferred fatty acid alkyl esters such as C 10 -C 22 -fatty acid C 1 -C 20 -alkyl esters are methyl esters, ethyl esters, propyl esters, butyl esters, 2-ethylhexyl esters and dodecyl esters.
  • Preferred glycol and glycerol fatty acid esters such as C 10 -C 22 -fatty acid esters are the uniform or mixed glycol esters and glycerol esters of C 10 -C 22 -fatty acids, in particular of such fatty acids having an even number of carbon atoms, for example erucic acid, lauric acid, palmitic acid and in particular C 18 -fatty acids such as stearic acid, oleic acid, linoleic acid or linolenic acid.
  • animal oils and vegetable oils are generally known and commercially available.
  • the term "animal oils” is to be understood as meaning oils of animal origin such as whale oil, cod-liver oil, musk oil or mink oil
  • the term “vegetable oils” is to be understood as meaning oils of oleaginous plant species, such as soybean oil, rapeseed oil, corn oil, sunflower oil, cottonseed oil, linseed oil, coconut oil, palm oil, thistle oil, walnut oil, arachis oil, olive oil or castor oil, in particular rapeseed oil, where the vegetable oils also include their transesterification products, for example alkyl esters, such as rapeseed oil methyl ester or rapeseed oil ethyl ester.
  • the vegetable oils are preferably esters of C 10 -C 22 -fatty acids, preferably C 12 -C 20 -fatty acids.
  • the C 10 -C 22 -fatty acid esters are, for example, esters of unsaturated or saturated C 10 -C 22 -fatty acids having, in particular, an even number of carbon atoms, for example erucic acid, lauric acid, palmitic acid and in particular C 18 -fatty acids such as stearic acid, oleic acid, linoleic acid or linolenic acid.
  • Examples of vegetable oils are C 10 -C 22 -fatty acid esters of glycerol or glycol with C 10 -C 22 -fatty acids, or C 10 -C 22 -fatty acid C 1 -C 20 -alkyl esters which can be obtained, for example, by transesterification of the glycerol or glycol C 10 -C 22 -fatty acid esters mentioned above with C 1 -C 20 -alcohols (for example methanol, ethanol, propanol or butanol).
  • C 1 -C 20 -alcohols for example methanol, ethanol, propanol or butanol.
  • the vegetable oils can be contained in the mixtures for example in the form of commercially available vegetable oils, in particular rapeseed oils, such as rapeseed oil methyl ester, for example Phytorob® B (Novance, France), Edenor® MESU and the Agnique® ME series (Cognis, Germany) the Radia® series (ICI), the Prilube® series (Petrofina), or biodiesel or in the form of commercially available plant-oil-containing formulation additives, in particular those based on rapeseed oils, such as rapeseed oil methyl esters, for example Hasten® (Victoria Chemical Company, Australia), Actirob® B (Novance, France), Rako-Binol® (Bayer AG, Germany), Renol® (Stefes, Germany) or Mero® (Stefes, Germany).
  • rapeseed oils such as rapeseed oil methyl ester
  • Phytorob® B Novance, France
  • Examples of synthetic acid esters are, for example, those derived from fatty acids having an odd number of carbon atoms, such as C 11 -C 21 -fatty acid esters.
  • Preferred organic solvents are hydrocarbons, in particular aromatic hydrocarbons and/or aliphatic hydrocarbons and fatty acid esters, such as vegetable oils, such as triglycerides of fatty acids having 10 to 22 carbon atoms, which may be saturated or else unsaturated, straight-chain or branched and which may or may not carry further functional groups, such as corn oil, rapeseed oil, sunflower oil, cottonseed oil, linseed oil, soybean oil, coconut oil, palm oil, thistle oil or castor oil, and their trans-esterification products, such as fatty acid alkyl esters, and mixtures thereof.
  • vegetable oils such as triglycerides of fatty acids having 10 to 22 carbon atoms, which may be saturated or else unsaturated, straight-chain or branched and which may or may not carry further functional groups, such as corn oil, rapeseed oil, sunflower oil, cottonseed oil, linseed oil, soybean oil, coconut oil, palm oil, thistle oil or castor oil
  • Preferred solvents for use in the present invention include: linear or branched C6 to C30 paraffin oils, for example hexane, heptane, octane, nonane, decane, undecane, dodecane, tridecane, tetradecane, pentadecane, hexadecane, their mixtures, or mixtures thereof with higher boiling homologs, such as hepta-, octa-, nona-decane, eicosane, heneicosane, docosane, tricosane, tetracosane, pentacosane, and the branched chain isomers thereof; aromatic or cycloaliphatic solvents, which may be unsubstituted or substituted, C7- to C18-hydrocarbon compounds such as mono- or polyalkyl-substituted benzenes, or mono- or polyalkyl-substituted
  • alkyl esters such as rapeseed oil methyl ester or rapeseed oil ethyl ester; animal oil, such as whale oil, cod-liver oil, or mink oil; liquid esters of C1 to C12 monoalcohols or polyols, for example butanol, n-octanol, i-octanol, dodecanol, cyclopentanol, cyclohexanol, cyclooctanol, ethylene glycol, propylene glycol or benzyl alcohol, with C2 to C10 carboxylic or polycarboxylic acids, such as caproic acid, capric acid, caprylic acid, pelargonic acid, succinic acid and glutaric acid; or with aromatic carboxylic acids such as benzoic acid, toluic acid, salicylic acid and phthalic acid.
  • animal oil such as whale oil, cod-liver oil, or mink oil
  • Esters which can be used in the composition of the invention are thus, for example, benzyl acetate, caproic acid ethyl ester, isobornyl acetate, pelargonic acid ethyl ester, benzoic acid methyl or ethyl ester, salicylic acid methyl, propyl, or butyl ester, diesters of phthalic acid with saturated aliphatic or alicyclic C1 to C12 alcohols, such as phthalic acid dimethyl ester, dibutyl ester, diisooctyl ester; liquid amides of C1-C3 amines, alkylamines or alkanolamines with C6 to C18 carboxylic acids; or mixtures thereof.
  • the non-aqueous solvent system is present in an amount such that it can act as a liquid carrier for the other components that are present in the composition.
  • the non-aqueous solvent system comprises an organic solvent in an amount of at least 5 wt.% based on the weight of the composition.
  • a low amount of organic solvent is possible when other components in the composition are also liquids (e.g. liquid herbicide and/or liquid emulsifier).
  • the non-aqueous solvent system comprises an organic solvent in an amount of at least 10 wt.%, at least 15 wt.%, at least 20 wt%, at least 25 wt%, at least 30 wt.%, or at least 40 wt.% of the composition.
  • the non-aqueous solvent system comprises an organic solvent in an amount of 95 wt.% or less of the composition. More preferably the non-aqueous solvent system comprises an organic solvent in an amount of 90 wt.% or less, 85 wt.% or less, 80 wt.% or less, 75 wt.% or less, or 60 wt.% or less of the composition. Any of the disclosed wt.% lower limits for the amount of the organic solvent in the non-aqueous solvent system can be combined with any of the disclosed wt.% upper limits to define further suitable wt.% ranges for the purpose of this invention.
  • exemplary ranges for the amount of the organic solvent in the composition include 5 to 95 wt.%, 10 to 90 wt.%, 20 to 80 wt.%, 30 to 60 wt.%, 40 to 60 wt.%, 10 to 75 wt.% and 20 to 60 wt.%.
  • the amounts described herein refer to the sum amount of all the organic solvents present in the composition.
  • the total amount of protic organic solvent such as alcohols, amines and carboxylic acids is preferably kept to 20 wt.% or less based on the weight of the liquid composition. More preferably, the total amount of protic organic solvent is 15 wt.% or less, 10 wt.% or less, 5 wt.% or less, 2 wt.% or less, or 1 wt.% or less of the composition.
  • the amounts described herein refer to the sum amount of all the protic solvents present in the composition.
  • the composition of the present invention may comprise one or more herbicides in addition to the sulfonylurea herbicide(s).
  • additional non-sulfonylurea herbicides may be liquids, waxy solids or powders and may be dissolved, dispersed, suspended or otherwise contained in the composition.
  • the additional herbicidal compound is not particularly limited and can be any herbicidal compound known in the art.
  • the compound may be selected from the herbicidal compounds listed in the 16th Edition of "The Pesticide Manual" (ISBN-10: 190139686X ) and the literature cited therein.
  • Exemplary additional herbicidal compounds include: 2,4-D (e.g.
  • the additional non-sulfonylurea herbicide is preferably comprised in the liquid composition of the invention in an amount of at least 0.1 wt.%. More preferably, the non-sulfonylurea herbicide is comprised in an amount of at least 0.2 wt.%, at least 0.5 wt.%, at least 0.7 wt.%, at least 1 wt.%, at least 2 wt.%, at least 5 wt.%, at least 10 wt.%, at least 15 wt.%, at least 20 wt.% or at least 25 wt.%. The non-sulfonylurea herbicide is preferably comprised in the composition an amount of 95 wt.% or less.
  • non-sulfonylurea herbicide is itself a liquid. More preferably, the non-sulfonylurea herbicide is comprised in an amount of 60 wt.% or less, 50 wt.% or less, 40 wt.% or less, 35 wt.% or less, 30 wt.% or less or 25 wt.% or less. Any of the disclosed wt.% lower limits for the amount of non-sulfonylurea herbicide can be combined with any of the disclosed wt.% upper limits to define further suitable wt.% ranges for the purposes of this invention.
  • further exemplary ranges for the amount of non-sulfonylurea herbicide in the liquid composition include 0.1 to 95 wt.%, 1 to 60 wt.%, 2 to 50 wt.%, 5 to 40 wt.%, 10 to 30 wt.%, 15 to 25 wt.%, 25 to 35 wt.% and 10 to 50 wt.%.
  • the wt.% amounts that are described herein refer to the weight of the salt or derivative.
  • the amounts described herein refer to the sum amount of all of the non-sulfonylurea herbicides present in the composition.
  • one or more of the non-sulfonylurea herbicides may be partially or wholly encapsulated (e.g. microcapsules) such as is described in WO 2008/061721 A2 (GAT Microencapsulation AG).
  • the wt.% amounts that are described herein refer to the weight of the non-sulfonylurea herbicides without the encapsulating material.
  • the liquid composition of the invention may comprise any of the sulfonylureas described herein with any of the non-sulfonylurea herbicides described herein.
  • the liquid composition may comprise tribenuron-methyl and any of the other non-sulfonylurea herbicides described herein.
  • Exemplary combinations with tribenuron-methyl include: tribenuron-methyl and 2,4-D (e.g. as ester or amine or choline salt); tribenuron methyl and MCPA (e.g. as ester or amine); tribenuron-methyl and bromoxynil; tribenuron-methyl and glyphosate; tribenuron-methyl and fluroxypyr; tribenuron-methyl and dicamba (e.g.
  • tribenuron-methyl and mecoprop-P tribenuron-methyl and MCPB
  • tribenuron-methyl and carfentrazone ethyl tribenuron-methyl and clopyralid (e.g. as MEA salt); tribenuron-methyl and clodinafop; tribenuron-methyl and quinclorac; tribenuron-methyl and florasulam.
  • the liquid composition may comprise nicosulfuron and any of the other non-sulfonylurea herbicides described herein.
  • nicosulfuron include: nicosulfuron and dicamba (optionally as the sodium salt or ester); nicosulfuron and atrazine; nicosulfuron and flumetsulam; nicosulfuron and clopyralid (optionally as the potassium salt or ester); nicosulfuron and diflupenzopyr (optionally as the sodium salt or ester); nicosulfuron and metolachlor; nicosulfuron and terbuthylazine; nicosulfuron and mesotrione; and nicosulfuron and bentazone.
  • the liquid composition may comprise metsulfuron-methyl and any of the other non-sulfonylurea herbicides described herein.
  • exemplary combinations with metsulfuron-methyl include: metsulfuron-methyl and acetochlor; metsulfuron-methyl and carfentrazone ethyl; metsulfuron-methyl and imazapyr; metsulfuron-methyl and aminopyralid; metsulfuron-methyl and fluroxypyr; metsulfuron-methyl and mecoprop-p; metsulfuron-methyl and picloram; metsulfuron-methyl and pyraflufen ethyl; metsulfuron-methyl and propanil; metsulfuron-methyl and glyphosate-ammonium; metsulfuron-methyl and dicamba (optionally as the sodium, dimethylammonium or diglycolamine salt or as an ester); metsulfuron-methyl and 2,4-D (optionally as the dimethylammonium salt
  • sulfonylureas and non-sulfonylureas for use in the present invention include: bensulfuron-methyl and acetochlor; bensulfuron-methyl and indanofan; bensulfuron-methyl and clomeprop; bensulfuron-methyl and pretilachlor; bensulfuron-methyl and fentrazamide; bensulfuron-methyl and thenylchlor; bensulfuron-methyl and pentoxazone; bensulfuron-methyl and pyriminobac-methyl; bensulfuron-methyl and bromobutide; bensulfuron-methyl, pentoxazone, pyriminobac-methyl, and bromobutide; bensulfuron-methyl and butachlor; bensulfuron-methyl and daimuron; bensulfuron-methyl and mefenacet; bensulfuron-methyl, daimur
  • pyrasulfuron-ethyl and pretilachlor pyrasulfuron-ethyl and pyriftalid; pyrasulfuron-ethyl and mefenacet; pyrasulfuron-ethyl and esprocarb; pyrasulfuron-ethyl and dimethametryn; pyrasulfuron-ethyl and oxaziclomefone; pyrasulfuron-ethyl and benzobicyclon; pyrasulfuron-ethyl and cyhalofop-butyl; pyrasulfuron-ethyl and penoxsulam; pyrasulfuron-ethyl, cyhalofop-butyl, pretilachlor, and dimethametryn; pyrasulfuron-ethyl, benzobicyclon and penoxsulam; pyrasulfuron-e
  • composition of the present invention may comprise one or more safeners that may be dissolved, dispersed, suspended or otherwise contained in the composition.
  • Suitable safeners are those listed in the " The Pesticide Manual” (ISBN-10: 190139686X ), as well as those listed in paragraphs [0113] to [0129] of US 2006/0276337 A1 , which paragraphs are incorporated herein by reference.
  • Exemplary safeners include:
  • Preferred herbicide safeners for use in the present invention include benoxacor, BCS (1-bromo-4-[(chloromethyl)sulfonyl]benzene), cloquintocet-mexyl, cyometrinil, cyprosulfamide, dichlormid, dicyclonon, 2-(dichloromethyl)-2-methyl-1,3-dioxolane (MG 191), dietholate, fenchlorazole-ethyl, fenclorim, flurazole, fluxofenim, furilazole, isoxadifen-ethyl, jiecaowan, jiecaoxi, mefenpyr, mefenpyrethyl, methoxyphenone ((4-methoxy-3-methylphenyl)(3-methylphenyl)methanone), mephenate, naphthalic anhydride and oxabetrinil.
  • the liquid composition of the invention may comprise any of the sulfonylureas described herein with any suitable safener described herein.
  • exemplary combinations of sulfonylurea and safener include: iodosulfuron-methyl (optionally as the sodium salt) and mefenpyr-diethyl; mesosulfuron (and/or as the methyl ester) and mefenpyr-di-ethyl; mesosulfuron (and/or as the methyl ester) and propoxycarbazone (e.g. sodium salt) and mefenpyr-di-ethyl.
  • the composition of the invention may comprise one or more additional co-formulants such as surfactants (e.g. emulsifiers and/or dispersants), thickeners and thixotropic agents, wetting agents, anti-drift agents, adhesives, penetrants, preservatives, antifreeze agents, antioxidants, solubilizers, fillers, carriers, colorants, antifoams, fertilizers, evaporation inhibitors and agents which modify pH and viscosity.
  • the liquid composition comprises at least one co-formulant that is an adjuvant, such as one of those listed in the Compendium of Herbicide Adjuvants, 12th Edition, Southern Illinois University, 2014 , or any earlier edition thereof.
  • adjuvants include, but are not limited to, paraffin oil, horticultural spray oils (e.g., summer oil), methylated rape seed oil, methylated soybean oil, highly refined vegetable oil and the like, polyol fatty acid esters, polyethoxylated esters, ethoxylated alcohols, alkyl polysaccharides and blends, amine ethoxylates, sorbitan fatty acid ester ethoxylates, polyethylene glycol esters, alkylpolyglucosides and their derivatives (e.g. esters), organosilicone based surfactants, ethylene vinyl acetate terpolymers, ethoxylated alkyl aryl phosphate esters and the like.
  • paraffin oil e.g., summer oil
  • methylated rape seed oil methylated soybean oil
  • highly refined vegetable oil and the like polyol fatty acid esters
  • polyethoxylated esters ethoxylated alcohols
  • the liquid composition of the invention includes one or more surfactants, for example, to enable the forming an emulsion if the compositions are to be diluted with water.
  • surfactants can be cationic, anionic or non-ionic, but are preferably anionic or non-ionic.
  • Preferred non-ionic surfactants for use in this invention include: polyalkoxylated, preferably polyethoxylated, saturated and unsaturated aliphatic alcohols having 8 to 24 carbon atoms in the alkyl radical, which is derived from the corresponding fatty acids or from petrochemical products, and having 1 to 100, preferably 2 to 50, ethylene oxide units (EO), it being possible for the free hydroxyl group to be alkoxylated, which are commercially available, for example, as Genapol® X and Genapol® O series (Clariant), Crovol® M series (Croda) or as Lutensol® series (BASF); polyalkoxylated, preferably polyethoxylated, arylalkylphenols, such as, for example, 2,4,6-tris(1-phenylethyl)phenol (tristyrylphenol) having an average degree of ethoxylation of between 10 and 80, preferably from 16 to 40, such as, for example, Soprophor® B
  • Preferred ionic surfactants for use in this invention include: polyalkoxylated, preferably polyethoxylated, surfactants which are ionically modified, for example by conversion of the terminal free hydroxyl function of the polyethylene oxide block into a sulfate or phosphate ester (for example as alkali metal and alkaline earth metal salts), such as, for example, Genapol® LRO or dispersant 3618 (Clariant), Emulphor® (BASF) or Crafol® AP (Cognis); alkali metal and alkaline earth metal salts of alkylarylsulfonic acids having a straight-chain or branched alkyl chain, such as phenylsulfonate CA or phenylsulfonate CAL (Clariant), Atlox® 3377BM (ICI), or the Empiphos® TM series (Huntsman); polyelectrolytes, such as lignosulfonates, condensates of n
  • OMS organo-modified siloxanes
  • GET Microencapsulation examples include those disclosed in the Compendium of Herbicide Adjuvants, 12th Edition, Southern Illinois University, 2014 , or any earlier edition thereof, as well as those disclosed in WO 2008/155108 A2 (GAT Microencapsulation), as well as the polyether-polysiloxane copolymers described in GB 2496643 (Rotam Agrochem), including those available from Evonik Industries under the trade names Break-Thru 9902TM, Break-Thru 9903TM, Break-Thru 5503TM, Break-Thru 9907TM and Break-Thru 9908TM.
  • OMS organo-modified siloxanes
  • the surfactant is preferably included in an amount of at least 1 wt.% with respect to the total weight of the composition. More preferably, the surfactant is comprised in an amount of at least 2 wt.%, at least 5 wt.%, at least 10 wt.%, at least 15 wt.%, or at least 20 wt.%. The surfactant is preferably comprised in the composition an amount of 60 wt.% or less. More preferably, the surfactant is comprised in an amount of 50 wt.% or less, 40 wt.% or less, or 30 wt.% or less.
  • any of the disclosed wt.% lower limits for the amount of surfactant can be combined with any of the disclosed wt.% upper limits to define further suitable wt.% ranges for the purposes of this invention.
  • further exemplary ranges for the amount of surfactant in the liquid composition include 1 to 60 wt.%, 2 to 50 wt.%, 5 to 40 wt.%, 10 to 30 wt.%, 5 to 50 wt.% and 2 to 40 wt.%. Where more than one surfactant is used the preferred ranges refer to the total amount of surfactant present in the liquid composition.
  • composition of the invention can be prepared by known processes, for example by mixing the components and milling the suspended solids or dissolving the solids.
  • Any soluble agrochemically active compounds used can also be dissolved in the premix.
  • solid sulfonylurea, any other insoluble agrochemically active compounds used and the inorganic salts can be suspended in the mixture.
  • the coarse suspension is, if appropriate after pregrinding, subjected to fine grinding.
  • solid sulfonylurea and, if appropriate, any insoluble components used are suspended in the non-aqueous solvent system and subjected to grinding. Any soluble active compounds used and any auxiliaries and additives which do not require grinding or are not required for the grinding process can be added after grinding.
  • customary mixing apparatus which, if required, are thermostatted.
  • pre-grinding it is possible to use, for example, high-pressure homogenizers or mills operating by the rotor-stator principle, such as Ultraturrax homogenizers, for example those from IKA, or toothed colloid mills, for example from Puck or Fryma.
  • Ultraturrax homogenizers for example those from IKA
  • toothed colloid mills for example from Puck or Fryma
  • fine grinding it is possible to use, for example, bead mills which operate batchwise, for example from Drais, or bead mills which operate continuously, for example from Bachofen or Eiger.
  • the invention is concerned with improving chemical stability of a sulfonylurea herbicide in liquid composition comprising a non-aqueous solvent system. Improved chemical stability may be achieved by including, in the liquid composition, at least one inorganic salt selected from the metal carbonates and metal phosphates.
  • the sulfonyl urea, the inorganic salt and the non-aqueous solvent system can be selected to meet desired needs such as to ensure that the liquid composition conforms with one or more local regulatory requirements.
  • the sulfonyl urea, the inorganic salt and the non-aqueous solvent system are selected such that the sulfonyl urea exhibits at least 85% chemical stability.
  • the sulfonyl urea exhibits at least 90% chemical stability, more preferably at least 95% chemical stability, and still more preferably at least 98% chemical stability.
  • Chemical stability can be determined as a percentage of the sulfonyl urea remaining (e.g. as determined by HPLC) when the liquid composition (e.g. a 50 ml sample of the liquid composition in a 60 ml hermetically sealed Winchester bottle) has been stored at 54°C for two weeks relative to a corresponding control sample that has been stored at -10°C for two weeks.
  • the liquid composition is one where chemical stability of the sulfonyl urea is improved by at least 2% compared to a corresponding liquid composition that does not contain an inorganic salt according to the invention (instead of salt, an equivalent extra wt.% of solvent is used).
  • Chemical stability of the sulfonylurea for each of the salt-containing liquid composition and the non-salt control composition can be determined as described immediately above. The difference in chemical stability can then be calculated to determine that an improvement of at least 2% is achieved.
  • the sulfonyl urea exhibits at least a 5% improvement, more preferably at least a 10% improvement, and even more preferably at least a 50% improvement in chemical stability.
  • the liquid composition is one where the sulfonyl urea exhibits at least 85% chemical stability (as described above), and is one where the chemical stability of the sulfonyl urea is improved by at least 10% compared to a corresponding liquid composition that does not contain an inorganic salt according to the invention (as described above).
  • the sulfonyl urea exhibits at least 90% chemical stability, more preferably at least 95% chemical stability, and even more preferably at least 98% chemical stability.
  • the chemical stability, or improvement thereon is determined based on the total amount of sulfonylurea herbicide in the composition.
  • composition of the invention can be applied directly or can be diluted with water and then applied to plant foliage and/or soil by methods commonly employed in the art, such as conventional high-volume hydraulic sprays, low-volume sprays, air-blast, and aerial sprays.
  • the diluted composition may be applied to the plant foliage or to the soil or area adjacent to the plant.
  • the selection of the specific herbicidal compounds in the composition (both sulfonylureas and non-sulfonylureas) and their rates and mode of application are determined by the selectivity of the herbicidal compounds to specific crops and by the prevalent weed species to be controlled and are known to those skilled in the art (e.g. see " The Pesticide Manual” (ISBN-10: 190139686X ) and all earlier editions thereof).
  • liquid compositions are as follows:
  • any of the exemplary embodiments (i) to (xxii) as listed above can be further modified in line with the general description provided herein.
  • the sum amount of sulfonylurea in any of the exemplary embodiments (i) to (xxii) can be from 1 to 50wt.%, 2 to 40 wt.%, 5 to 30 wt.%, 0.5 to 20 wt.%, 7 to 30 wt.%, and 5 to 10 wt.%.
  • the total amount of inorganic salt selected from the metal phosphates and metal carbonates that is present in the exemplary embodiments (i) to (xxii) can be from 0.1 to 25 wt.%, 1 to 20 wt.%, 1 to 10 wt.%, 0.5 to 10 wt.%, 1 to 5 wt.% and 0.5 to 5 wt.%.
  • the weight ratio of the total amount of inorganic salt selected from the metal phosphates and metal carbonates inorganic salt to the total amount of sulfonylurea can be from 0.2 to 4, 0.3 to 3, 0.5 to 2, 0.7 to 2, 0.1 to 2, 1 to 2 and 1 to 5.
  • any of the exemplary embodiments (i), (vi), or (xi) can further comprise fluroxypyr-meptyl as a non-sulfonylurea.
  • the exemplary embodiments (i), (vi), (xi) (xvi), (xvii), (xviii), (xx), (xxi) or (xxii) comprise metsulfuron-methyl and fluroxypyr-meptyl.
  • the exemplary embodiments (i), (vi), (xi) (xvi), (xvii), (xviii), (xx), (xxi) or (xxii) comprise metsulfuron-methyl (optionally as the sodium salt), fluroxypyr-meptyl, Na 3 PO 4 and isobornyl acetate.
  • the exemplary embodiments (i), (vi), (xi) (xvi), (xvii), (xviii), (xx), (xxi) or (xxii) comprise 0.5 to 2 wt.% metsulfuron-methyl (optionally as the sodium salt), 25 to 35 wt.% fluroxypyr-meptyl, 0.2 to 1 wt.% Na 3 PO 4 and 40-60 wt.% isobornyl acetate. Any of the exemplary embodiments (i) to (xxii) or as described herein can further comprise a surfactant and/or a safener.
  • oil dispersions described in the following examples were prepared as follows.
  • Sulfonylurea was added to a solvent in an amount of 25 wt.%.
  • the mixture was placed in a mill (Eiger Torrance Mini Mill) containing glass beads (1.0-1.25 mm).
  • the suspension was then milled to provide a 25 wt.% sulfonylurea millbase having a particle size (D50) between 2 and 3 ⁇ m.
  • Inorganic salt (anhydrous) was added to solvent in an amount of 30 wt.% and milled as described above to provide a 30 wt.% inorganic salt millbase having a particle size (D50) between 2 and 3 ⁇ m.
  • a polymeric dispersant Atlox LP1
  • Emulsifiable concentrates were prepared by blending the milled concentrate of sulfonylurea (i) with surfactant in a solvent and blending this with an appropriate amount of the milled concentrate of salt (ii).
  • liquid formulations were stored in tightly closed glass bottles in thermostatically controlled incubators at 54°C for two weeks with control samples stored at -10°C. After storage, all formulations were analysed for active ingredient content(s) by HPLC. Stability is reported with respect to the amount of active ingredient remaining relative to a corresponding sample stored at - 10°C for two weeks.
  • Example 2 Improved stability of different sulfonylureas
  • sulfonylureas having comparatively high stability (nicosulfuron), medium stability (metsulfuron methyl) and low stability (tribenuron-methyl) were chosen for this example.
  • the relative stability of the three chosen sulfonylureas is reflected in the stability data for OD18-OD21. If an inorganic salt selected from the metal carbonates and metal phosphates (OD12-OD17) is included in the oil dispersion, the chemical stability of the sulfonylurea can be greatly improved.
  • the very low stability of sulfonylureas such as tribenuron-methyl has limited their widespread use in liquid compositions. This problem is overcome by the present invention.
  • the addition of a non-sulfonylurea co-herbicide greatly reduces the stability of the sulfonylurea (OD28-OD30).
  • the addition of an inorganic salt selected from the metal carbonates and metal phosphates greatly improves the chemical stability of the sulfonylurea even in the presence of a co-herbicide.
  • the present invention overcomes the problem and opens up the opportunity for a multiplicity of novel liquid formulations of sulfonylureas co-formulated with non-sulfonylurea herbicides.
  • the sulfonylurea is stabilised by the inorganic salt irrespective of the emulsifier that is used (OD31-OD35) and also when no emulsifier is used (OD36; see also OD2). Contrary to the liquid compositions described in WO 2008/155108 A2 and WO2009/152827 A2 which require very specific emulsifier systems, a sulfonylurea-containing liquid composition with co-formulated inorganic salt in accordance with the present invention is stable for a wide range of emulsifying systems.
  • EC emulsifiable concentrate
  • Table 7 Example Comparative Example EC1 EC2 Components (wt.%) metsulfuron-methyl 5 5 Na 3 PO 4 2.5 Soprophor BSU 20 20 Atlox LP1 0.02 Isobornyl acetate 20.83 23.33 n-butylpyrrolidone 51.65 51.67 Stability (%) 92.0 0
  • Table 8-1 demonstrates that not only can an inorganic salt selected from the metal carbonates and metal phosphates stabilise a comparatively low-stable sulfonylurea in an emulsifiable concentrate, the sulfonylurea is stabilised in a wide range of solvent systems, including one comprising a pyrrolidone solvent.
  • Example 9 Improved chemical stability with Mg 3 (PO 4 ) 2 or AlPO 4
  • Example 10 Improved chemical stability of different sulfonylureas with Na 3 PO 4
  • Example 11 -Urea as a chemical stabilizer for Nicosulfuron and Tribenuron-methyl
  • EP 0554015 A1 (Ishihara Sangyo Kaisha) teaches that urea can be used to stabilise nicosulfuron (referred to as "Compound A” in that document).
  • Oil dispersions comprising nicosulfuron were prepared and tested to determine the chemical stability of the sulfonylurea after storage at 60°C for one week (same ageing test as used in EP 0554015 A1 ). Stability is reported with respect to the amount of active ingredient remaining as determined by HPLC relative to a corresponding sample stored at -10°C for one week. The results are summarised in Table 11 below.
  • a liquid composition comprising a sulfonyl urea in a non-aqueous solvent system (dimethyl sulfoxide) was prepared with and without an added salt and tested.
  • the sulfonylurea was dissolved in the DMSO and the salt (milled) was dispersed as solid particles.
  • Table 12 Examples Comparative Example 12-1 12-2 12-3 Components (wt.%) tribenuron - methyl 5 5 5 Na 3 PO 4 5 5 5 Soprophor BSU 10 20 10 DMSO 80 70 85 Stability (%) 97.1 96.4 0

Landscapes

  • Life Sciences & Earth Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Wood Science & Technology (AREA)
  • Environmental Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Dentistry (AREA)
  • Pest Control & Pesticides (AREA)
  • Agronomy & Crop Science (AREA)
  • Zoology (AREA)
  • Plant Pathology (AREA)
  • Chemical & Material Sciences (AREA)
  • Inorganic Chemistry (AREA)
  • Toxicology (AREA)
  • Dispersion Chemistry (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)
  • Catching Or Destruction (AREA)
EP18170343.0A 2014-12-22 2015-12-21 Compositions herbicides contenant du sulfonylurea liquide Active EP3387904B1 (fr)

Priority Applications (1)

Application Number Priority Date Filing Date Title
PL18170343T PL3387904T3 (pl) 2014-12-22 2015-12-21 Ciekłe kompozycje chwastobójcze zawierające sulfonylomocznik

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
EP14199867 2014-12-22
EP15813079.9A EP3236749B1 (fr) 2014-12-22 2015-12-21 Compositions herbicides contenant du tribenuron liquide
PCT/EP2015/080844 WO2016102499A1 (fr) 2014-12-22 2015-12-21 Compositions herbicides liquides contenant de la sulfonylurée

Related Parent Applications (2)

Application Number Title Priority Date Filing Date
EP15813079.9A Division-Into EP3236749B1 (fr) 2014-12-22 2015-12-21 Compositions herbicides contenant du tribenuron liquide
EP15813079.9A Division EP3236749B1 (fr) 2014-12-22 2015-12-21 Compositions herbicides contenant du tribenuron liquide

Publications (2)

Publication Number Publication Date
EP3387904A1 true EP3387904A1 (fr) 2018-10-17
EP3387904B1 EP3387904B1 (fr) 2019-12-18

Family

ID=52134029

Family Applications (3)

Application Number Title Priority Date Filing Date
EP18170343.0A Active EP3387904B1 (fr) 2014-12-22 2015-12-21 Compositions herbicides contenant du sulfonylurea liquide
EP18203057.7A Pending EP3456199A1 (fr) 2014-12-22 2015-12-21 Compositions herbicides contenant du sulfonylurea liquide
EP15813079.9A Active EP3236749B1 (fr) 2014-12-22 2015-12-21 Compositions herbicides contenant du tribenuron liquide

Family Applications After (2)

Application Number Title Priority Date Filing Date
EP18203057.7A Pending EP3456199A1 (fr) 2014-12-22 2015-12-21 Compositions herbicides contenant du sulfonylurea liquide
EP15813079.9A Active EP3236749B1 (fr) 2014-12-22 2015-12-21 Compositions herbicides contenant du tribenuron liquide

Country Status (18)

Country Link
US (2) US11071296B2 (fr)
EP (3) EP3387904B1 (fr)
JP (1) JP6736560B6 (fr)
KR (1) KR102291873B1 (fr)
CN (3) CN107427010B (fr)
AU (1) AU2015371074B2 (fr)
BR (1) BR112017013448B1 (fr)
CA (1) CA2971795C (fr)
CO (1) CO2017006981A2 (fr)
DK (1) DK3236749T3 (fr)
EA (1) EA038316B1 (fr)
ES (2) ES2739540T3 (fr)
HU (2) HUE048629T2 (fr)
MX (1) MX2017008371A (fr)
PL (2) PL3387904T3 (fr)
TR (1) TR201910889T4 (fr)
UA (1) UA122330C2 (fr)
WO (1) WO2016102499A1 (fr)

Families Citing this family (20)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN107427010B (zh) 2014-12-22 2020-07-17 三井农业化学国际有限公司 液态含磺酰脲的除草性组合物
FR3046179A1 (fr) * 2015-12-23 2017-06-30 Oleon Nv Composition dispersante
DE102016210164A1 (de) * 2016-06-08 2017-12-14 Clariant International Ltd Verwendung von N-substituierten Pyrrolidonen zur Förderung der Penetration von agrochemischen Wirkstoffen
CA3018651C (fr) * 2016-06-21 2019-06-04 Battelle Uk Limited Compositions herbicides contenant de la sulfonyluree liquide et du sel de li
EP3664604A4 (fr) * 2017-08-11 2021-05-19 Arysta Lifescience Inc. Composition herbicide et procédé
TWI702000B (zh) * 2017-11-16 2020-08-21 南韓商Ｌｇ化學股份有限公司 液體除草組成物
TWI713933B (zh) * 2017-11-16 2020-12-21 南韓商Ｌｇ化學股份有限公司 液體除草組成物
TWI722335B (zh) * 2017-11-16 2021-03-21 南韓商Ｌｇ化學股份有限公司 除草組成物
CN107960422A (zh) * 2017-12-06 2018-04-27 江苏省农业科学院 一种一次施药防控稻茬小麦全生育期草害的除草剂减量控草方法
CN108041043A (zh) * 2018-02-02 2018-05-18 陕西上格之路生物科学有限公司 一种含吡氟酰草胺的三元除草组合物
CN108308187A (zh) * 2018-02-11 2018-07-24 河北中天邦正生物科技股份公司 一种农药组合物及其应用
WO2020172305A1 (fr) 2019-02-19 2020-08-27 Gowan Company, L.L.C. Compositions liquides stables et leurs procédés d'utilisation
RU2714736C1 (ru) * 2019-04-02 2020-02-19 Общество с ограниченной ответственностью "АХК-АГРО" Гербицидная композиция
WO2020234175A1 (fr) 2019-05-21 2020-11-26 Syngenta Crop Protection Ag Compositions améliorées de dispersion d'huile herbicide
WO2021152391A1 (fr) 2020-01-29 2021-08-05 Fmc Agricultural Caribe Industries Ltd. Compositions de sulfonylurée liquides
EP3900535A1 (fr) 2020-04-24 2021-10-27 Battelle UK Limited Composition herbicide de sulfonylurée liquide
CN112400876A (zh) * 2020-11-24 2021-02-26 安徽苏昆化工科技有限公司 一种包含仲丁灵、苄嘧磺隆和丁草胺的除草组合物
CN112262848A (zh) * 2020-11-24 2021-01-26 安徽苏昆化工科技有限公司 一种包含仲丁灵、吡嘧磺隆和丁草胺的除草组合物
RU2771039C1 (ru) * 2021-08-05 2022-04-25 ООО "Агро Эксперт Груп" Жидкая гербицидная композиция
WO2023058040A1 (fr) * 2021-10-08 2023-04-13 Aviral Crop Science Pvt. Ltd. Composition herbicide ternaire

Citations (33)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2059773A (en) 1979-10-12 1981-04-29 Boots Co Ltd Fungicidal compositions
EP0086750A2 (fr) 1982-02-17 1983-08-24 Ciba-Geigy Ag Utilisation de dérivés de la quinoléine pour la protection de plantes cultivables
EP0094349A2 (fr) 1982-05-07 1983-11-16 Ciba-Geigy Ag Utilisation de dérivés de quinoléine pour protéger des plantes cultivées
EP0124295A2 (fr) 1983-04-04 1984-11-07 E.I. Du Pont De Nemours And Company Formulations aqueuses stabilisées de sulfonylurées
JPS6087254A (ja) 1983-10-19 1985-05-16 Japan Carlit Co Ltd:The 新規尿素化合物及びそれを含有する除草剤
EP0174562A2 (fr) 1984-09-11 1986-03-19 Hoechst Aktiengesellschaft Agents pour la protection de plantes basés sur des dérivés de 1,2,4- briazole ainsi que dérivés 1,2,4-triazole
EP0191736A2 (fr) 1985-02-14 1986-08-20 Ciba-Geigy Ag Utilisation de dérivés de la quinoléine pour la protection de plantes cultivables
EP0269806A1 (fr) 1986-10-04 1988-06-08 Hoechst Aktiengesellschaft Dérivés d'acide phénylpyrazolcarbonique, leur préparation et leur utilisation comme agents régulateurs de croissance des plantes et antidote
EP0333131A1 (fr) 1988-03-17 1989-09-20 Hoechst Aktiengesellschaft Agent de protection des plantes à base de dérivés d'acide pyrazolcarboxylique
EP0346620A1 (fr) 1988-05-20 1989-12-20 Hoechst Aktiengesellschaft Agents phytoprotecteurs contenant des dérivés du 1,2,4-triazole ainsi que dérivés du 1,2,4-triazole
WO1991008202A1 (fr) 1989-11-25 1991-06-13 Hoechst Aktiengesellschaft Isoxazolines, procede de preparation et application comme produits phytosanitaires
WO1991007874A1 (fr) 1989-11-30 1991-06-13 Hoechst Aktiengesellschaft Pyrazoline pour la protection de plantes cultivees contre les herbicides
EP0492366A2 (fr) 1990-12-21 1992-07-01 Hoechst Schering AgrEvo GmbH Nouveaux dérivés de chloro-5-quinoline-8-acide oxyalkanecarboniques, procédé pour leur préparation et leur utilisation comme antidote d'herbicides
WO1993013658A1 (fr) 1992-01-06 1993-07-22 E.I. Du Pont De Nemours And Company Composition de comprime comportant un agent deshydratant incorpore
EP0554015A1 (fr) 1992-01-28 1993-08-04 Ishihara Sangyo Kaisha, Ltd. Suspension herbicide à base d'huile chimiquement stabilisée
EP0582198A2 (fr) 1992-08-01 1994-02-09 Hoechst Schering AgrEvo GmbH Composés (hétéro-)aryliques substitués, procédé pour leur préparation, compositions les contenant et leur utilisation comme agents de protection
WO1995007897A1 (fr) 1993-09-16 1995-03-23 Hoechst Schering Agrevo Gmbh Isoxazolines substituees, leur procede de preparation, agents les contenant et leur utilisation comme reducteurs de phytotoxicite
EP0764404A1 (fr) 1995-09-21 1997-03-26 Ishihara Sangyo Kaisha, Ltd. Composition granulaire herbicide
US5707928A (en) 1993-09-28 1998-01-13 American Cyanamid Company Emulsifiable suspension concentrate compositions of imidazolinyl benzoic acids, esters and salts thereof, and dinitroaniline herbicides
US5731264A (en) 1996-10-17 1998-03-24 Isp Investments Inc. Stabilized liquid emulsifiable concentrate for a sulfonyl or sulfamoylurea herbicide
WO1998034482A1 (fr) 1997-02-05 1998-08-13 Basf Aktiengesellschaft Melanges solides a base de sulfonylurees et adjuvants
WO2002017718A1 (fr) 2000-08-31 2002-03-07 Basf Aktiengesellschaft Procede de preparation d'une composition herbicide solide
WO2003051114A1 (fr) 2001-12-18 2003-06-26 Isp Investments Inc. Prolongement de la duree de conservation de microemulsions contenant un biocide aza actif
US20050113254A1 (en) 2003-11-03 2005-05-26 Bayer Cropscience Gmbh Herbicidally active composition
US20060276337A1 (en) 2005-06-04 2006-12-07 Bayer Cropscience Gmbh Oil suspension concentrate
WO2007027863A2 (fr) 2005-09-01 2007-03-08 E. I. Du Pont De Nemours And Company Formulations herbicides sulfonyluree liquides
WO2008061721A2 (fr) 2006-11-23 2008-05-29 Gat Microencapsulation, Ag Nouvelles formulations agrochimiques contenant des microcapsules
WO2008155108A2 (fr) 2007-06-19 2008-12-24 Gat Microencapsulation, Ag Suspensions huileuses de sulfonylurées et de combinaisons agrochimiques
WO2009152827A2 (fr) 2008-05-28 2009-12-23 Gat Microencapsulation, Ag Suspensions concentrées dans de l'huile de sulfonylurées et combinaisons avec du fluroxypyr ou d'autres produits agrochimiques
WO2012175899A1 (fr) 2011-06-23 2012-12-27 Syngenta Limited Composition herbicide comprenant un herbicide pyranedione et un herbicide sulfonylurée
GB2496643A (en) 2011-11-17 2013-05-22 Rotam Agrochem Int Co Ltd Herbicidal suspension concentrate
WO2013174833A1 (fr) 2012-05-25 2013-11-28 Bayer Cropscience Ag Stabilisation chimique de sel de iodosulfuron-méthyle-sodium par des hydroxystéarates
WO2014018410A1 (fr) 2012-07-24 2014-01-30 Dow Agrosciences Llc Compositions herbicides comprenant de l'acide 4-amino-3-chloro-5-fluoro-6-(4-chloro-2-fluoro-3-méthoxyphényl)pyridine-2-carboxylique

Family Cites Families (30)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA915702A (en) 1970-05-21 1972-11-28 Eric Lucien Preparation of 1-benzene-sulfonyl-3-hydrocarbylureas and derivatives
US4579583A (en) 1982-09-08 1986-04-01 Ciba-Geigy Corporation Novel sulfonylureas
WO1984003903A1 (fr) 1983-03-31 1984-10-11 Robert Edward Silman Procede et dispositif pour detecter des micro-organismes
US4936900A (en) 1983-04-04 1990-06-26 E. I. Du Pont De Nemours And Company Stabilized aqueous formulations of sulfonylurea salts
US4599412A (en) 1983-11-23 1986-07-08 E. I. Du Pont De Nemours And Company Process for preparation of sulfonylurea solution formulations
ATE104825T1 (de) 1989-09-21 1994-05-15 Du Pont Stabilisierung von nichtwaessrigen suspensionen.
JPH05188793A (ja) * 1992-01-09 1993-07-30 Canon Inc 画像形成装置
AU3801793A (en) 1992-05-12 1993-12-13 Church & Dwight Company, Inc. Herbicide compositions
DE69411583T2 (de) 1993-11-15 1999-02-18 Zeneca Ltd Mikrokapseln, die suspensionen von biologisch aktiven verbindungen enthalten
CN1159881A (zh) 1996-03-14 1997-09-24 化学工业部沈阳化工研究院 磺酰脲类除草混剂
CN1181880A (zh) 1996-11-12 1998-05-20 湖南化工研究院 水稻秧田和直播田除草剂系列组合物
CA2272319A1 (fr) 1996-11-22 1998-05-28 E.I. Du Pont De Nemours And Company Sels d'ammonium quaternaire et leur utilisation dans des formulations a usage agricole
JP4189612B2 (ja) 1998-09-24 2008-12-03 日産化学工業株式会社 安定化する懸濁除草製剤
AU1802100A (en) 1999-01-07 2000-07-24 Ishihara Sangyo Kaisha Ltd. Floating pesticide compositions for paddy fields, method for the utilization thereof and process for producing the same
AR030412A1 (es) 2000-03-22 2003-08-20 Fmc Corp Proceso novedoso para preparar formulaciones acuosas
AR030664A1 (es) 2000-09-13 2003-08-27 Basf Ag Suspensiones oleosas concentradas a base de una sal de litio de ciclohexenonaximeter y su uso como composiciones firoprotectoras
US20040023876A1 (en) * 2000-10-31 2004-02-05 Yonghong Xiao Regulation of human serotonin receptor precursor
WO2002062138A2 (fr) 2001-02-02 2002-08-15 E. I. Du Pont De Nemours And Company Procede de lutte contre les plantes nuisibles dans une culture de laitue
AR041211A1 (es) * 2002-09-12 2005-05-11 Du Pont Procedimiento para preparar composiciones de sulfonamida extruidas en pasta
KR100491579B1 (ko) * 2003-07-01 2005-05-27 삼성전자주식회사 화상형성장치의 인쇄용지 잼 판단 방법
DE10334301A1 (de) 2003-07-28 2005-03-03 Bayer Cropscience Gmbh Flüssige Formulierung
JP5137348B2 (ja) 2005-08-10 2013-02-06 石原産業株式会社 水性懸濁状除草組成物
SA06270491B1 (ar) * 2005-12-27 2010-10-20 سينجنتا بارتيسبيشنز ايه جي تركيبة مبيدة للأعشاب تشتمل على حمض 2، 2- ثنائي ميثيل بروبيونيك 8- (2، 6- ثنائي إيثيل –4- ميثيل – فينيل) –9- أوكسو –1، 2، 4، 5- تتراهيدرو –9h- بيرازولو[2.1-دي][ 5.4.1] أوكسادايازيبين –7- يل إستر وكحول
GB0712884D0 (en) * 2007-07-03 2007-08-15 Syngenta Ltd Formulations
AU2011248750B2 (en) * 2010-04-26 2015-04-30 Corteva Agriscience Llc Stabilized agricultural oil dispersions
US8962004B2 (en) * 2011-04-05 2015-02-24 Arysta Lifescience North America, Llc Encapsulated triazinyl sulfonylurea herbicide and methods of use
CN103371160A (zh) * 2012-04-27 2013-10-30 龙灯农业化工国际有限公司 一种降低药物残留的农药组合物
WO2015089104A1 (fr) * 2013-12-09 2015-06-18 Oms Investments, Inc. Substrats contenant un herbicide sulfonylurée et leurs procédés de fabrication
CN107427010B (zh) 2014-12-22 2020-07-17 三井农业化学国际有限公司 液态含磺酰脲的除草性组合物
CA3018651C (fr) * 2016-06-21 2019-06-04 Battelle Uk Limited Compositions herbicides contenant de la sulfonyluree liquide et du sel de li

Patent Citations (33)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2059773A (en) 1979-10-12 1981-04-29 Boots Co Ltd Fungicidal compositions
EP0086750A2 (fr) 1982-02-17 1983-08-24 Ciba-Geigy Ag Utilisation de dérivés de la quinoléine pour la protection de plantes cultivables
EP0094349A2 (fr) 1982-05-07 1983-11-16 Ciba-Geigy Ag Utilisation de dérivés de quinoléine pour protéger des plantes cultivées
EP0124295A2 (fr) 1983-04-04 1984-11-07 E.I. Du Pont De Nemours And Company Formulations aqueuses stabilisées de sulfonylurées
JPS6087254A (ja) 1983-10-19 1985-05-16 Japan Carlit Co Ltd:The 新規尿素化合物及びそれを含有する除草剤
EP0174562A2 (fr) 1984-09-11 1986-03-19 Hoechst Aktiengesellschaft Agents pour la protection de plantes basés sur des dérivés de 1,2,4- briazole ainsi que dérivés 1,2,4-triazole
EP0191736A2 (fr) 1985-02-14 1986-08-20 Ciba-Geigy Ag Utilisation de dérivés de la quinoléine pour la protection de plantes cultivables
EP0269806A1 (fr) 1986-10-04 1988-06-08 Hoechst Aktiengesellschaft Dérivés d'acide phénylpyrazolcarbonique, leur préparation et leur utilisation comme agents régulateurs de croissance des plantes et antidote
EP0333131A1 (fr) 1988-03-17 1989-09-20 Hoechst Aktiengesellschaft Agent de protection des plantes à base de dérivés d'acide pyrazolcarboxylique
EP0346620A1 (fr) 1988-05-20 1989-12-20 Hoechst Aktiengesellschaft Agents phytoprotecteurs contenant des dérivés du 1,2,4-triazole ainsi que dérivés du 1,2,4-triazole
WO1991008202A1 (fr) 1989-11-25 1991-06-13 Hoechst Aktiengesellschaft Isoxazolines, procede de preparation et application comme produits phytosanitaires
WO1991007874A1 (fr) 1989-11-30 1991-06-13 Hoechst Aktiengesellschaft Pyrazoline pour la protection de plantes cultivees contre les herbicides
EP0492366A2 (fr) 1990-12-21 1992-07-01 Hoechst Schering AgrEvo GmbH Nouveaux dérivés de chloro-5-quinoline-8-acide oxyalkanecarboniques, procédé pour leur préparation et leur utilisation comme antidote d'herbicides
WO1993013658A1 (fr) 1992-01-06 1993-07-22 E.I. Du Pont De Nemours And Company Composition de comprime comportant un agent deshydratant incorpore
EP0554015A1 (fr) 1992-01-28 1993-08-04 Ishihara Sangyo Kaisha, Ltd. Suspension herbicide à base d'huile chimiquement stabilisée
EP0582198A2 (fr) 1992-08-01 1994-02-09 Hoechst Schering AgrEvo GmbH Composés (hétéro-)aryliques substitués, procédé pour leur préparation, compositions les contenant et leur utilisation comme agents de protection
WO1995007897A1 (fr) 1993-09-16 1995-03-23 Hoechst Schering Agrevo Gmbh Isoxazolines substituees, leur procede de preparation, agents les contenant et leur utilisation comme reducteurs de phytotoxicite
US5707928A (en) 1993-09-28 1998-01-13 American Cyanamid Company Emulsifiable suspension concentrate compositions of imidazolinyl benzoic acids, esters and salts thereof, and dinitroaniline herbicides
EP0764404A1 (fr) 1995-09-21 1997-03-26 Ishihara Sangyo Kaisha, Ltd. Composition granulaire herbicide
US5731264A (en) 1996-10-17 1998-03-24 Isp Investments Inc. Stabilized liquid emulsifiable concentrate for a sulfonyl or sulfamoylurea herbicide
WO1998034482A1 (fr) 1997-02-05 1998-08-13 Basf Aktiengesellschaft Melanges solides a base de sulfonylurees et adjuvants
WO2002017718A1 (fr) 2000-08-31 2002-03-07 Basf Aktiengesellschaft Procede de preparation d'une composition herbicide solide
WO2003051114A1 (fr) 2001-12-18 2003-06-26 Isp Investments Inc. Prolongement de la duree de conservation de microemulsions contenant un biocide aza actif
US20050113254A1 (en) 2003-11-03 2005-05-26 Bayer Cropscience Gmbh Herbicidally active composition
US20060276337A1 (en) 2005-06-04 2006-12-07 Bayer Cropscience Gmbh Oil suspension concentrate
WO2007027863A2 (fr) 2005-09-01 2007-03-08 E. I. Du Pont De Nemours And Company Formulations herbicides sulfonyluree liquides
WO2008061721A2 (fr) 2006-11-23 2008-05-29 Gat Microencapsulation, Ag Nouvelles formulations agrochimiques contenant des microcapsules
WO2008155108A2 (fr) 2007-06-19 2008-12-24 Gat Microencapsulation, Ag Suspensions huileuses de sulfonylurées et de combinaisons agrochimiques
WO2009152827A2 (fr) 2008-05-28 2009-12-23 Gat Microencapsulation, Ag Suspensions concentrées dans de l'huile de sulfonylurées et combinaisons avec du fluroxypyr ou d'autres produits agrochimiques
WO2012175899A1 (fr) 2011-06-23 2012-12-27 Syngenta Limited Composition herbicide comprenant un herbicide pyranedione et un herbicide sulfonylurée
GB2496643A (en) 2011-11-17 2013-05-22 Rotam Agrochem Int Co Ltd Herbicidal suspension concentrate
WO2013174833A1 (fr) 2012-05-25 2013-11-28 Bayer Cropscience Ag Stabilisation chimique de sel de iodosulfuron-méthyle-sodium par des hydroxystéarates
WO2014018410A1 (fr) 2012-07-24 2014-01-30 Dow Agrosciences Llc Compositions herbicides comprenant de l'acide 4-amino-3-chloro-5-fluoro-6-(4-chloro-2-fluoro-3-méthoxyphényl)pyridine-2-carboxylique

Non-Patent Citations (5)

* Cited by examiner, † Cited by third party
Title
"Compendium of Herbicide Adjuvants, 12th Edition,", 2014, SOUTHERN ILLINOIS UNIVERSITY
"Technical Monograph", 2008, CROPLIFE INTERNATIONAL, article "Catalogue of pesticide formulation types and international coding system"
.: "The Pesticide Manual 16th edition", ISBN: 190139686X
ALAN KNOWLES: "New Trends in Crop Protection Formulations", 2013
WADE VAN VALKENBURG, PESTICIDE FORMULATIONS, 1973

Also Published As

Publication number Publication date
MX2017008371A (es) 2018-04-30
ES2778998T3 (es) 2020-08-13
CN111713504A (zh) 2020-09-29
CO2017006981A2 (es) 2017-10-10
HUE048629T2 (hu) 2020-08-28
EP3236749A1 (fr) 2017-11-01
CA2971795C (fr) 2021-02-09
AU2015371074A1 (en) 2017-07-27
US20210137102A1 (en) 2021-05-13
WO2016102499A1 (fr) 2016-06-30
JP2018502109A (ja) 2018-01-25
CA2971795A1 (fr) 2016-06-30
KR102291873B1 (ko) 2021-08-20
PL3236749T3 (pl) 2019-11-29
US11071296B2 (en) 2021-07-27
EA201791345A1 (ru) 2018-01-31
JP6736560B2 (ja) 2020-08-05
AU2015371074B2 (en) 2019-05-02
UA122330C2 (uk) 2020-10-26
CN107427010A (zh) 2017-12-01
TR201910889T4 (tr) 2019-08-21
EA038316B1 (ru) 2021-08-09
PL3387904T3 (pl) 2020-08-10
EP3236749B1 (fr) 2019-07-03
CN107427010B (zh) 2020-07-17
EP3456199A1 (fr) 2019-03-20
ES2739540T3 (es) 2020-01-31
JP6736560B6 (ja) 2023-03-22
CN111631226A (zh) 2020-09-08
HUE044475T2 (hu) 2019-10-28
DK3236749T3 (da) 2019-08-05
KR20170105530A (ko) 2017-09-19
EP3387904B1 (fr) 2019-12-18
BR112017013448B1 (pt) 2021-09-28
BR112017013448A2 (pt) 2018-01-09
US20180000069A1 (en) 2018-01-04

Similar Documents

Publication Publication Date Title
EP3236749B1 (fr) Compositions herbicides contenant du tribenuron liquide
EP3416486B1 (fr) Compositions liquides herbicides contenant un sel de sulfonylurée et de li
EP3236750A1 (fr) Dispersion huileuse herbicide
EP4138556B1 (fr) Composition herbicide de sulfonylurée liquide

Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: THE APPLICATION HAS BEEN PUBLISHED

AC Divisional application: reference to earlier application

Ref document number: 3236749

Country of ref document: EP

Kind code of ref document: P

AK Designated contracting states

Kind code of ref document: A1

Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: REQUEST FOR EXAMINATION WAS MADE

17P Request for examination filed

Effective date: 20190321

RBV Designated contracting states (corrected)

Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: EXAMINATION IS IN PROGRESS

17Q First examination report despatched

Effective date: 20190603

GRAP Despatch of communication of intention to grant a patent

Free format text: ORIGINAL CODE: EPIDOSNIGR1

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: GRANT OF PATENT IS INTENDED

INTG Intention to grant announced

Effective date: 20190813

GRAS Grant fee paid

Free format text: ORIGINAL CODE: EPIDOSNIGR3

GRAA (expected) grant

Free format text: ORIGINAL CODE: 0009210

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: THE PATENT HAS BEEN GRANTED

AC Divisional application: reference to earlier application

Ref document number: 3236749

Country of ref document: EP

Kind code of ref document: P

AK Designated contracting states

Kind code of ref document: B1

Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR

REG Reference to a national code

Ref country code: CH

Ref legal event code: EP

REG Reference to a national code

Ref country code: DE

Ref legal event code: R096

Ref document number: 602015044122

Country of ref document: DE

REG Reference to a national code

Ref country code: IE

Ref legal event code: FG4D

REG Reference to a national code

Ref country code: AT

Ref legal event code: REF

Ref document number: 1213556

Country of ref document: AT

Kind code of ref document: T

Effective date: 20200115

REG Reference to a national code

Ref country code: RO

Ref legal event code: EPE

REG Reference to a national code

Ref country code: NL

Ref legal event code: FP

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: GR

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20200319

Ref country code: NO

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20200318

Ref country code: LT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20191218

Ref country code: SE

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20191218

Ref country code: LV

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20191218

Ref country code: FI

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20191218

REG Reference to a national code

Ref country code: LT

Ref legal event code: MG4D

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: RS

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20191218

Ref country code: HR

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20191218

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: AL

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20191218

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: EE

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20191218

Ref country code: PT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20200513

Ref country code: CZ

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20191218

REG Reference to a national code

Ref country code: CH

Ref legal event code: PL

REG Reference to a national code

Ref country code: ES

Ref legal event code: FG2A

Ref document number: 2778998

Country of ref document: ES

Kind code of ref document: T3

Effective date: 20200813

REG Reference to a national code

Ref country code: HU

Ref legal event code: AG4A

Ref document number: E048629

Country of ref document: HU

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: SM

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20191218

Ref country code: SK

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20191218

Ref country code: IS

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20200418

REG Reference to a national code

Ref country code: DE

Ref legal event code: R097

Ref document number: 602015044122

Country of ref document: DE

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: MC

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20191218

REG Reference to a national code

Ref country code: AT

Ref legal event code: MK05

Ref document number: 1213556

Country of ref document: AT

Kind code of ref document: T

Effective date: 20191218

PLBE No opposition filed within time limit

Free format text: ORIGINAL CODE: 0009261

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: NO OPPOSITION FILED WITHIN TIME LIMIT

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: DK

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20191218

Ref country code: LU

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20191221

26N No opposition filed

Effective date: 20200921

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: LI

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20191231

Ref country code: SI

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20191218

Ref country code: CH

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20191231

Ref country code: AT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20191218

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: CY

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20191218

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: MT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20191218

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: TR

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20191218

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: MK

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20191218

REG Reference to a national code

Ref country code: HU

Ref legal event code: HC9C

Owner name: MITSUI AGRISCIENCE INTERNATIONAL S.A./N.V., IE

Free format text: FORMER OWNER(S): MITSUI AGRISCIENCE INTERNATIONAL S.A./N.V., IE

Ref country code: HU

Ref legal event code: HC9C

Owner name: BATTELLE UK LIMITED, GB

Free format text: FORMER OWNER(S): MITSUI AGRISCIENCE INTERNATIONAL S.A./N.V., IE

REG Reference to a national code

Ref country code: DE

Ref legal event code: R081

Ref document number: 602015044122

Country of ref document: DE

Owner name: MITSUI AGRISCIENCE INTERNATIONAL S.A./N.V., BE

Free format text: FORMER OWNERS: BATTELLE UK LTD., CHELMSFORD, ESSEX, GB; MITSUI AGRISCIENCE INTERNATIONAL S.A./N.V., DUBLIN, IE

Ref country code: DE

Ref legal event code: R081

Ref document number: 602015044122

Country of ref document: DE

Owner name: BATTELLE UK LTD., CHELMSFORD, GB

Free format text: FORMER OWNERS: BATTELLE UK LTD., CHELMSFORD, ESSEX, GB; MITSUI AGRISCIENCE INTERNATIONAL S.A./N.V., DUBLIN, IE

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: GB

Payment date: 20231208

Year of fee payment: 9

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: RO

Payment date: 20231206

Year of fee payment: 9

Ref country code: NL

Payment date: 20231211

Year of fee payment: 9

Ref country code: IT

Payment date: 20231221

Year of fee payment: 9

Ref country code: IE

Payment date: 20231115

Year of fee payment: 9

Ref country code: HU

Payment date: 20231124

Year of fee payment: 9

Ref country code: FR

Payment date: 20231219

Year of fee payment: 9

Ref country code: DE

Payment date: 20231206

Year of fee payment: 9

Ref country code: BG

Payment date: 20231115

Year of fee payment: 9

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: PL

Payment date: 20231211

Year of fee payment: 9

Ref country code: BE

Payment date: 20231211

Year of fee payment: 9

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: ES

Payment date: 20240102

Year of fee payment: 9